London, UK
Posted: Sep 08, 2024
RemoteFull-time
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Skills Required
Biopharma
expert
Clinical Research
Proficient
Pharmaceutical
Proficient
Nice To Have skills
Job Description
You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.

You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.


Amongst other tasks, your main responsibilities will be to;

  • Contribute to the selection of potential investigators.
  • Provide the required monitoring visit reports within required timelines
  • Drive performance at the sites. Proactively identify study-related issues and escalate as appropriate.
  • Perform source data verification according to SDV plan and ensure data query resolution
  • Initiate, monitor and close study sites in compliance with client Procedural Documents. Share information on patient recruitment and study site progress within local Study Delivery Team.
  • Train, support and advise Investigators and site staff in study related matters.
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Additional Info
Min. Experience
-
Job Location Type
Remote
Job Type
Full-time
Predicted Seniority Level
-
Job Duration
-
Language(s)
English
Est. Budget/Pay Rate
To be discussed
Est. hrs
-
Optimal Job Start
-
Job Industry
-
Job Function
-
Employer
ICON
Preferred Applicant Countries
United Kingdom
Job Ref
J24A8AA5A700C
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